Last synced on 14 June 2024 at 11:05 pm

pRESET Thrombectomy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222848
510(k) Type
Traditional
Applicant
phenox Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
1/20/2023
Days to Decision
121 days
Submission Type
Summary

pRESET Thrombectomy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222848
510(k) Type
Traditional
Applicant
phenox Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
1/20/2023
Days to Decision
121 days
Submission Type
Summary